List of variants in gene FGB reported as other by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005141.4(FGB):c.1433G>A (p.Arg478Lys)	rs4220	0.15295
NM_005141.4(FGB):c.220C>T (p.Arg74Cys)	rs121909619	0.00001
FIBRINOGEN NEW YORK 1
NM_005141.4(FGB):c.1093G>A (p.Ala365Thr)	rs121909617
NM_005141.4(FGB):c.130C>T (p.Arg44Cys)	rs121909616
NM_005141.4(FGB):c.133G>T (p.Gly45Cys)	rs121909618
NM_005141.4(FGB):c.292G>A (p.Ala98Thr)	rs121909620
NM_005141.4(FGB):c.586C>T (p.Arg196Cys)	rs121909623

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